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The Journal of Neurophysiology Vol. 87 No. 3 March 2002, pp. 1415-1425
Copyright ©2002 by the American Physiological Society
1Freie Universität Berlin, Fachbereich Biologie, Chemie, Pharmazie, Institut für Biologie (Neurobiologie), D-14195 Berlin, Germany; and 2Division of Neurobiology, University of Arizona, Tucson, Arizona 85721
Duch, C. and
R. B. Levine.
Changes in Calcium Signaling During Postembryonic Dendritic
Growth in Manduca sexta. J. Neurophysiol. 87: 1415-1425, 2002. Activity-dependent
Ca2+ influx plays crucial roles in adult and
developing nervous systems through its influence on signal processing, synaptic plasticity, and neuronal differentiation. The responses to
internal Ca2+ elevations vary depending on the
spatial distribution of Ca2+ accumulation in
different cell compartments. In this study, the mechanisms and the
distribution of Ca2+ accumulation are addressed
by in situ Ca2+ imaging of an identified insect
motoneuron, MN5, at critical stages of postembryonic life. During
metamorphosis of Manduca sexta, MN5 undergoes extensive
dendritic regression followed by regrowth. The time course, amplitude,
and distribution of Ca2+ accumulation within MN5
change during development. During the initial stage of rapid dendritic
growth and branching, dendritic growth cones are present, and
voltage-dependent Ca2+ currents are small. At
this stage, activity-induced elevations of internal
Ca2+ are largest in the distal dendrites,
suggesting that the density of voltage-gated Ca2+
channels is highest in these regions. Later phases of dendritic growth
are accompanied by the transient occurrence of prominent Ca2+ spikes. Single Ca2+
spikes cause robust Ca2+ influx of similar
amplitudes and time courses in all central compartments of MN5. The
resting Ca2+ levels also increase during
development. Ca2+-induced
Ca2+ release from intracellular stores did not
contribute to the elevations measured at either stage, although
Ca2+ stores are present in the dendrites. These
developmental changes of the internal Ca2+
signaling are consistent with a regulatory role for activity-dependent Ca2+ influx in postembryonic dendritic growth.
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